Flying With Diabetes.

I love to travel.  I by no means travel more than some of my PWD (people with diabetes) friends but I have to been numerous locations abroad in recent years.  (Usually nice, warm, sunny locations!)  Lucky for me, the great people over at Sanofi Diabetes asked if I was willing to share some advice or tips if you will, on traveling with diabetes.  I am very honored to be featured over there today 🙂

Flying with Diabetes: Tips from Stacey Divone

Giving.

Since becoming active in the diabetes online community over the past couple of years, I have found a profound admiration for the parents of children with diabetes.  I was once a child with diabetes however never got to see what my parents went through from their perspective.  But now I can, through their voices.  One of those parents is Scott Benner. He has been a stay-at-home father since his son, Cole, was born in early 2000. His daughter, Arden, was diagnosed with type I diabetes just after her second birthday, in the summer of 2006. Exactly one year later, he wrote his first blog post on his site, www.ardensday.com.  Scott has something new up his sleeve and I wanted to share with all of you so please read on.

 

What do you get the best damn retweeter in the diabetes online community for the holidays? I’m seriously asking because all I got for Stacey was more words to show to other people. There are a few folks in the DOC that I could never thank enough for their support and the Girl with the Portable Pancreas is definitely one of them.

Let me get to the point before you start asking yourself why Stacey gave me this space today. Insulin pumps and continuous glucose monitors (CGMs) are expensive. Even the insured can lack the funds necessary to begin using these amazing devices because of large out of pocket costs. This single issue has long bothered me and I have written about it many times on my site, Arden’s Day. I’ve been trying for more then two years to find a way to put pumps and CGMs in the hands of children that want but can not afford them. I’ve spent countless hours trying to convince those who are in a position to help, that they should – but I’ve had very little success. I almost gave up when I realized that it wasn’t my goal that was faulty but my execution. I was asking the wrong people for help…

The diabetes online community is powerful, maybe more so then any one of it’s parts is aware. When we band together, we aren’t just powerful, we are unavoidable. I’ve seen it in the past, I’ve seen an entity bend to the will of the few. I can’t mention when or who because taking down my petition was part of the agreement that we made when said entity decided to listen. Please trust me, our voices have power.

A number of weeks ago I stopped hoping that I could get devices for children with type I diabetes for free and I turned my attention to finding the money to buy them for the kids myself. I struck an agreement with one device company to purchase their device at cost and with that agreement in place, I am moving forward to set up a charitable organization so that I can fundraise and begin the work.

Starting a charity is expensive, more expensive then my family could bear on it’s own. I had two choices, give up or do something bold. I chose bold. In just a few days amazing gifts have flooded my inbox to support the formation of this dream. They’ve come from all around the world, from North Carolina, Canada and even Finland. They have come in all sizes and types but each with the same sentiment. I am humbled and ready to pledge my time and my heart to making this dream a reality. If you’ve ever had the same thought, that diabetes devices should be available to every child that wants one, please take a few moments to find out more about my so far Untitled Giving Project.

My family is fortunate to have good insurance and the means to cover our out of pocket expenses. I want, almost as much as I want a cure for type I, to help the kids who aren’t – can you please consider helping me to help them?
My fondest regards, Scott @ArdensDay

Thank you Scott firstly, for what you are working on.  And secondly, for taking the time to share your generous efforts here with my readers.  I sincerely hope you will attain your goal and make the difference in the lives of children with diabetes!

Please visit http://www.ardensday.com/ardens-day-gives to make a donation.

Guest Post.

I met Sysy this past spring at the Diabetes Sisters Weekend for Women conference in Raleigh, NC.  I’m very glad I did 🙂

Being that she has children of her own (two beautiful twins mind you) she had asked me to provide a post on the perspective of being a woman with diabetes and not having children.  It was a hard one to write but I did want to share that with everyone.  I’m honored to have my post over at The Girl’s Guide to Diabetes today. 

A Type 1’s Decision Not to Have Children 

Thank you so much Sysy for the opportunity to write for you!